Lista de obras - Juho Wedenoja - Dominio Público Uruguay

A population-specific HTR2B stop codon predisposes to severe impulsivity

artículo científico publicado en 2010

Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits

artículo científico publicado en 2012

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins

artículo científico publicado en 2009

Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample

artículo científico publicado en 2008

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?

artículo científico publicado en 2012

Erratum: A population-specific HTR2B stop codon predisposes to severe impulsivity

scientific article published in Nature

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

article

Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

article

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

artículo científico publicado en 2016

Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2.

artículo científico publicado en 2016

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

artículo científico publicado en 2018

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

artículo científico publicado en 2020

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

artículo científico publicado en 2014

Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample

scientific article published on 11 June 2013

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

artículo científico publicado en 2012

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

artículo científico publicado en 2013

Genome-wide meta-analysis identifies new susceptibility loci for migraine

artículo científico publicado en 2013

Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene

artículo científico publicado en 2018

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

artículo científico publicado en 2016

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

artículo científico publicado en 2015

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

artículo científico publicado en 2015

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

artículo científico publicado en 2016

Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia

artículo científico publicado en 2009

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

artículo científico publicado en 2013

Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia

artículo científico publicado en 2010

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families

artículo científico publicado en 2007

Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder

artículo científico publicado en 2014

The role of vision-related problems in fatal road accidents in Finland

artículo científico publicado en 2020

Lista de obras de Juho Wedenoja

A population-specific HTR2B stop codon predisposes to severe impulsivity

Analysis of detailed phenotype profiles reveals CHRNA5-CHRNA3-CHRNB4 gene cluster association with several nicotine dependence traits

Analysis of shared heritability in common disorders of the brain

Association of AKT1 with verbal learning, verbal memory, and regional cortical gray matter density in twins

Association of a nonsynonymous variant of DAOA with visuospatial ability in a bipolar family sample

Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Does originating from a genetic isolate affect the level of cognitive impairments in schizophrenia families?

Erratum: A population-specific HTR2B stop codon predisposes to severe impulsivity

Erratum: Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms and neuroticism identified through genome-wide analyses

Erratum: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses

Genome-Wide Meta-Analysis of Cotinine Levels in Cigarette Smokers Identifies Locus at 4q13.2.

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error

Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error

Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: the CREAM consortium

Genome-wide association study on detailed profiles of smoking behavior and nicotine dependence in a twin sample

Genome-wide association study to identify common variants associated with brachial circumference: a meta-analysis of 14 cohorts

Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia

Genome-wide meta-analysis identifies new susceptibility loci for migraine

Keratoendotheliitis Fugax Hereditaria: A Novel Cryopyrin-Associated Periodic Syndrome Caused by a Mutation in the Nucleotide-Binding Domain, Leucine-Rich Repeat Family, Pyrin Domain-Containing 3 (NLRP3) Gene

Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium

Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder

Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error

Mixture model clustering of phenotype features reveals evidence for association of DTNBP1 to a specific subtype of schizophrenia

Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error

Replication of association between working memory and Reelin, a potential modifier gene in schizophrenia

Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families

Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder

The role of vision-related problems in fatal road accidents in Finland